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For: Gialluisi A, Visconti A, Willcutt EG, Smith SD, Pennington BF, Falchi M, DeFries JC, Olson RK, Francks C, Fisher SE. Investigating the effects of copy number variants on reading and language performance. J Neurodev Disord 2016;8:17. [PMID: 27186239 DOI: 10.1186/s11689-016-9147-8] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 2.3] [Reference Citation Analysis]
Number Citing Articles
1 Doust C, Fontanillas P, Eising E, Gordon SD, Wang Z, Alagöz G, Molz B, Pourcain BS, Francks C, Marioni RE, Zhao J, Paracchini S, Talcott JB, Monaco AP, Stein JF, Gruen JR, Olson RK, Willcutt EG, DeFries JC, Pennington BF, Smith SD, Wright MJ, Martin NG, Auton A, Bates TC, Fisher SE, Luciano M; 23andMe Research Team., Quantitative Trait Working Group of the GenLang Consortium. Discovery of 42 genome-wide significant loci associated with dyslexia. Nat Genet 2022. [PMID: 36266505 DOI: 10.1038/s41588-022-01192-y] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Moreno Campos V, Benítez-Burraco A. Communication deficits in a case of a deletion in 7q31.1-q31.33 encompassing FOXP2. Clin Linguist Phon 2022;:1-14. [PMID: 35702019 DOI: 10.1080/02699206.2022.2085174] [Reference Citation Analysis]
3 Doust C, Fontanillas P, Eising E, Gordon SD, Wang Z, Alagöz G, Molz B, Pourcain BS, Francks C, Marioni RE, Zhao J, Paracchini S, Talcott JB, Monaco AP, Stein JF, Gruen JR, Olson RK, Willcutt EG, Defries JC, Pennington BF, Smith SD, Wright MJ, Martin NG, Auton A, Bates TC, Fisher SE, Luciano M, 23andMe Research Team, Quantitative Trait Working Group of the GenLang Consortium. Discovery of 42 Genome-Wide Significant Loci Associated with Dyslexia.. [DOI: 10.1101/2021.08.20.21262334] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 4.5] [Reference Citation Analysis]
4 Georgitsi M, Dermitzakis I, Soumelidou E, Bonti E. The Polygenic Nature and Complex Genetic Architecture of Specific Learning Disorder. Brain Sci 2021;11:631. [PMID: 34068951 DOI: 10.3390/brainsci11050631] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
5 Gialluisi A, Andlauer TFM, Mirza-schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, Pourcain BS, Honbolygó F, Tóth D, Csépe V, Huguet G, Chaix Y, Iannuzzi S, Demonet J, Morris AP, Hulslander J, Willcutt EG, Defries JC, Olson RK, Smith SD, Pennington BF, Vaessen A, Maurer U, Lyytinen H, Peyrard-janvid M, Leppänen PHT, Brandeis D, Bonte M, Stein JF, Talcott JB, Fauchereau F, Wilcke A, Kirsten H, Müller B, Francks C, Bourgeron T, Monaco AP, Ramus F, Landerl K, Kere J, Scerri TS, Paracchini S, Fisher SE, Schumacher J, Nöthen MM, Müller-myhsok B, Schulte-körne G. Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. Mol Psychiatry. [DOI: 10.1038/s41380-020-00898-x] [Cited by in Crossref: 19] [Cited by in F6Publishing: 26] [Article Influence: 6.3] [Reference Citation Analysis]
6 Thygesen JH, Presman A, Harju-seppänen J, Irizar H, Jones R, Kuchenbaecker K, Lin K, Alizadeh BZ, Austin-zimmerman I, Bartels-velthuis A, Bhat A, Bruggeman R, Cahn W, Calafato S, Crespo-facorro B, de Haan L, de Zwarte SMC, Di Forti M, Díez-revuelta Á, Hall J, Hall M, Iyegbe C, Jablensky A, Kahn R, Kalaydjieva L, Kravariti E, Lawrie S, Luykx JJ, Mata I, Mcdonald C, Mcintosh AM, Mcquillin A, Muir R, Ophoff R, Picchioni M, Prata DP, Ranlund S, Rujescu D, Rutten BPF, Schulze K, Shaikh M, Schirmbeck F, Simons CJP, Toulopoulou T, van Amelsvoort T, van Haren N, van Os J, van Winkel R, Vassos E, Walshe M, Weisbrod M, Zartaloudi E, Bell V, Powell J, Lewis CM, Murray RM, Bramon E. Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study. Mol Psychiatry. [DOI: 10.1038/s41380-020-0820-7] [Cited by in Crossref: 7] [Cited by in F6Publishing: 11] [Article Influence: 2.3] [Reference Citation Analysis]
7 Bieder A, Einarsdottir E, Matsson H, Nilsson HE, Eisfeldt J, Dragomir A, Paucar M, Granberg T, Li T, Lindstrand A, Kere J, Tapia-páez I. Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia.. [DOI: 10.1101/2020.03.30.011783] [Reference Citation Analysis]
8 Price KM, Wigg KG, Feng Y, Blokland K, Wilkinson M, He G, Kerr EN, Carter TC, Guger SL, Lovett MW, Strug LJ, Barr CL. Genome-wide association study of word reading: Overlap with risk genes for neurodevelopmental disorders. Genes Brain Behav 2020;19:e12648. [PMID: 32108986 DOI: 10.1111/gbb.12648] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 5.0] [Reference Citation Analysis]
9 Tang H, Tang Y, Zeng T, Chen L. Gene expression analysis reveals the tipping points during infant brain development for human and chimpanzee. BMC Genomics 2020;21:74. [PMID: 32138647 DOI: 10.1186/s12864-020-6465-8] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
10 Felix RA 2nd, Chavez VA, Novicio DM, Morley BJ, Portfors CV. Nicotinic acetylcholine receptor subunit α7-knockout mice exhibit degraded auditory temporal processing. J Neurophysiol 2019;122:451-65. [PMID: 31116647 DOI: 10.1152/jn.00170.2019] [Cited by in Crossref: 13] [Cited by in F6Publishing: 15] [Article Influence: 3.3] [Reference Citation Analysis]
11 Park KB, Nam KE, Cho AR, Jang W, Kim M, Park JH. Effects of Copy Number Variations on Developmental Aspects of Children With Delayed Development. Ann Rehabil Med 2019;43:215-23. [PMID: 31072088 DOI: 10.5535/arm.2019.43.2.215] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Peter B, Dinu V, Liu L, Huentelman M, Naymik M, Lancaster H, Vose C, Schrauwen I. Exome Sequencing of Two Siblings with Sporadic Autism Spectrum Disorder and Severe Speech Sound Disorder Suggests Pleiotropic and Complex Effects. Behav Genet 2019;49:399-414. [DOI: 10.1007/s10519-019-09957-8] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 2.8] [Reference Citation Analysis]
13 Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, St Pourcain B, Brandler W, Honbolygó F, Tóth D, Csépe V, Huguet G, Morris AP, Hulslander J, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Vaessen A, Maurer U, Lyytinen H, Peyrard-Janvid M, Leppänen PHT, Brandeis D, Bonte M, Stein JF, Talcott JB, Fauchereau F, Wilcke A, Francks C, Bourgeron T, Monaco AP, Ramus F, Landerl K, Kere J, Scerri TS, Paracchini S, Fisher SE, Schumacher J, Nöthen MM, Müller-Myhsok B, Schulte-Körne G. Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Transl Psychiatry 2019;9:77. [PMID: 30741946 DOI: 10.1038/s41398-019-0402-0] [Cited by in Crossref: 56] [Cited by in F6Publishing: 57] [Article Influence: 14.0] [Reference Citation Analysis]
14 Kalnak N, Stamouli S, Peyrard-Janvid M, Rabkina I, Becker M, Klingberg T, Kere J, Forssberg H, Tammimies K. Enrichment of rare copy number variation in children with developmental language disorder. Clin Genet 2018;94:313-20. [PMID: 29851021 DOI: 10.1111/cge.13389] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 2.0] [Reference Citation Analysis]
15 Gialluisi A, Andlauer TFM, Mirza-schreiber N, Moll K, Hoffmann P, Ludwig KU, Czamara D, Francks C, St Pourcain B, Brandler W, Honbolygó F, Tóth D, Csépe V, Huguet G, Morris AP, Hulslander J, Willcutt EG, Defries JC, Olson RK, Smith SD, Pennington BF, Vaessen A, Maurer U, Lyytinen H, Peyrard-janvid M, Leppänen PHT, Brandeis D, Bonte M, Stein JF, Talcott JB, Fauchereau F, Bourgeron T, Monaco AP, Ramus F, Landerl K, Kere J, Scerri TS, Paracchini S, Fisher SE, Schumacher J, Nöthen MM, Müller-myhsok B, Schulte-körne G. Genome Wide Association Scan identifies new variants associated with a cognitive predictor of dyslexia.. [DOI: 10.1101/309336] [Reference Citation Analysis]
16 Becker N, Vasconcelos M, Oliveira V, Santos FCD, Bizarro L, Almeida RMM, Salles JF, Carvalho MRS. Genetic and environmental risk factors for developmental dyslexia in children: systematic review of the last decade. Dev Neuropsychol 2017;42:423-45. [PMID: 29068706 DOI: 10.1080/87565641.2017.1374960] [Cited by in Crossref: 28] [Cited by in F6Publishing: 18] [Article Influence: 4.7] [Reference Citation Analysis]
17 Deriziotis P, Fisher SE. Speech and Language: Translating the Genome. Trends in Genetics 2017;33:642-56. [DOI: 10.1016/j.tig.2017.07.002] [Cited by in Crossref: 42] [Cited by in F6Publishing: 45] [Article Influence: 7.0] [Reference Citation Analysis]